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Campo DC | Valor | Lengua/Idioma |
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dc.contributor.author | Soto, María Elena | - |
dc.contributor.author | Soria Castro, Elizabeth | - |
dc.contributor.author | Guarner Lans, Verónica | - |
dc.contributor.author | Martínez Guzmán, Andrés | - |
dc.contributor.author | Morales Marín, Cesar Amilcar | - |
dc.contributor.author | Martínez Zavala, Karla Susana | - |
dc.contributor.author | Pérez Torres, Israel | - |
dc.date.accessioned | 2022-10-26T15:46:25Z | - |
dc.date.available | 2022-10-26T15:46:25Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Histology and Histopathology Vol. 34, nº 12 (2019) | es |
dc.identifier.issn | 0213-3911 | - |
dc.identifier.issn | 1699-5848 | - |
dc.identifier.uri | http://hdl.handle.net/10201/124907 | - |
dc.description.abstract | Marfan syndrome (MS) is an autosomal dominant disorder of connective tissue that is caused by mutations in the fibrillin-1 (FBN-1) gene that cause degeneration of the artery. It is accompanied by endothelial dysfunction. The potential transient receptor of the vanilloid subfamily 1 (TRPV1) ion channel plays an important role in endothelial vascular functioning. Here we determine the association of the presence TRPV1 in aortic aneurysm with dilation and dissection of the artery in MS patients. Histological sections of aortic aneurysm tissue obtained by the surgical procedure of Bentall and De Bono or David, were processed by immunohistochemistry with antibodies against ICAM, VCAM, iNOS, eNOS, TRPV1 and TNF- α and the immunolabelling area was determined. We also measured the NO 3- /NO 2- ratio in the aortic tissue. C-reactive protein and HDL in plasma were quantified. A significant increase in iNOS, TRPV1, VCAM (p≤0.05), NO 3- /NO 2- ratio (p=0.002) and a significant decrease in eNOS (p=0.04) and HDL in plasma (p=0.02) in the MS vs. the C group were found. Conclusion: TRPV1 is over-expressed in aortic tissue from MS patients and can be associated with increases in iNOS, VCAM and a decrease in eNOS. These changes might contribute to the progression and rupture of the thoracic aneurysm. | es |
dc.format | application/pdf | es |
dc.format.extent | 15 | es |
dc.language | eng | es |
dc.publisher | Universidad de Murcia, Departamento de Biologia Celular e Histiologia | es |
dc.relation | Sin financiación externa a la Universidad | es |
dc.rights | info:eu-repo/semantics/openAccess | es |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Marfan syndrome | es |
dc.subject | TRPV1 | es |
dc.subject | eNOS | es |
dc.subject | iNOS | es |
dc.subject | Thoracic aneurysm | es |
dc.subject.other | CDU::6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncología | es |
dc.title | Preliminary analysis of the association of TRPV1 to the formation of Marfan syndrome aneurysms | es |
dc.type | info:eu-repo/semantics/article | es |
dc.identifier.doi | https://doi.org/10.14670/HH-18-127 | - |
Aparece en las colecciones: | Vol.34,nº12 (2019) |
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Soto-34-1329-1343-2019.pdf | 19,5 MB | Adobe PDF | Visualizar/Abrir |
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